Magnetoresistance of Manganese-Doped Colloidal Quantum Dot Films
Source abstract
Abstract
The magnetoresistance of films of manganese-doped colloidal quantum dots of CdSe, ZnO, HgS, and ZnTe is investigated. At low concentration of manganese ions (1% or less), the hyperfine splitting of the Mn 2+ electron spin resonance is resolved and similar to that of the bulk doped materials, indicating successful doping into the nanocrystals. At high Mn concentration (∼10%), the hyperfine splitting disappears because of interaction between the Mn 2+ ions. Thin films of Mn:CdSe, Mn:ZnO, and Mn:HgS quantum dots are charged negative by applying an electrochemical potential, and the magnetoresistance is measured down to 2 K and up to 9 T. At low charging level, the magnetoresistance of thin films is positive, exhibits little effect of the manganese dopant, and is instead consistent with predictions from the variable range hopping model and the squeezing of the wave function of the quantum dots. At high charging level, the magnetoresistance becomes linear both for Mn:CdSe and Mn:ZnO, and this is not explained. At high Mn doping and low temperature, the positive magnetoresistance is greatly increased at low fields. This is proposed to be a signature of electron-magnetic polarons on the transport properties of the quantum dot films.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Quantum Dots Synthesis And Properties · Semiconductor Quantum Structures and Devices · Quantum and electron transport phenomena
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
James Franck Institute, The University of Chicago, 929 East 57th Street, Chicago, Illinois 60637, United States
Funding
Basic Energy Sciences
References (40)
Show source-provided references
1. Furdyna J. K. · J. Appl. Phys. · 1988 · 64 · R2910.1063/1.341700 ↗
2. Story T. · Phys. Rev. Lett. · 1986 · 56 · 77710.1103/PhysRevLett.56.777 ↗
3. Matsukura F. · Phys. Rev. B: Condens. Matter Mater. Phys. · 1998 · 57 · R203710.1103/PhysRevB.57.R2037 ↗
4. Dietl T. · Nat. Mater. · 2010 · 9 · 96510.1038/nmat2898 ↗
5. Wolf S. A. · Science · 2011 · 294 · 148810.1126/science.1065389 ↗
6. Zutic I. · Rev. Mod. Phys. · 2004 · 76 · 32310.1103/RevModPhys.76.323 ↗
7. Bhattacharjee A. K. · Phys. Rev. B: Condens. Matter Mater. Phys. · 1997 · 55 · 1061310.1103/PhysRevB.55.10613 ↗
8. Beaulac R. · Adv. Funct. Mater. · 2008 · 18 · 387310.1002/adfm.200801016 ↗
9. Bacher G. · J. Korean Phys. Soc. · 2011 · 58 · 126110.3938/jkps.58.1261 ↗
10. Ochsenbein S. T. · Nat. Nanotechnol. · 2009 · 4 · 68110.1038/nnano.2009.221 ↗
11. Kaminski A. P. · Phys. Rev. Lett. · 2002 · 88 · 24720210.1103/PhysRevLett.88.247202 ↗
12. Yu D. · Appl. Phys. Lett. · 2006 · 88 · 07250410.1063/1.2174089 ↗
13. Pandey, A.Electronic Relaxation in Semiconductor Nanostructures. Ph.D. Thesis,The University of Chicago,Chicago, IL, 2009.
14. Zheng W. W. · J. Am. Chem. Soc. · 2011 · 133 · 748210.1021/ja200508e ↗
15. Archer P. I. · J. Am. Chem. Soc. · 2007 · 129 · 980810.1021/ja072436l ↗
16. Norris D. J. · Nano Lett. · 2000 · 1 · 310.1021/nl005503h ↗
17. Guyot-Sionnest P. · J. Phys. Chem. B · 2003 · 107 · 735510.1021/jp0275084 ↗
18. Pourret A. · Appl. Phys. Lett. · 2009 · 95 · 14210510.1063/1.3246157 ↗
19. Erwin S. C. · Nature · 2005 · 436 · 9110.1038/nature03832 ↗
20. Vanwieringen J. S. · Discuss. Faraday Soc. · 1955 · 19 · 11810.1039/df9551900118 ↗
21. Matumura O. · J. Phys. Soc. Jpn. · 1959 · 14 · 10810.1143/JPSJ.14.108 ↗
22. Mikulec F. V. · J. Am. Chem. Soc. · 2000 · 122 · 253210.1021/ja991249n ↗
23. Eilers J. · J. Phys. Chem. Lett. · 2012 · 3 · 166310.1021/jz300300g ↗
24. Vlaskin V. A. · J. Am. Chem. Soc. · 2013 · 135 · 1438010.1021/ja4072207 ↗
25. Liu H. · ACS Nano · 2010 · 4 · 521110.1021/nn101376u ↗
26. Shklovskii B. I. · Pis’ma Zh. Eksp. Teor. Fiz · 1982 · 36 · 43
27. Shklovskii B. I. · Sov. Phys. Semicond. · 1983 · 17 · 1311
28. Kapitza P. · Proc. R. Soc. London, Ser. A · 1929 · 123 · 29210.1098/rspa.1929.0072 ↗
29. Hu J. · Phys. Rev. Lett. · 2005 · 95 · 18660310.1103/PhysRevLett.95.186603 ↗
30. Friedman A. L. · Nano Lett. · 2010 · 10 · 396210.1021/nl101797d ↗
31. Wang X. · Phys. Rev. Lett. · 2012 · 108 · 26680610.1103/PhysRevLett.108.266806 ↗
32. Johnson H. G. · Phys. Rev. B: Condens. Matter Mater. Phys. · 2010 · 82 · 08520210.1103/PhysRevB.82.085202 ↗
33. Abrikosov A. A. · Phys. Rev. B: Condens. Matter Mater. Phys. · 1998 · 58 · 278810.1103/PhysRevB.58.2788 ↗
34. Parish M. M. · Nature · 2003 · 426 · 16210.1038/nature02073 ↗
35. Dietl T. · 1991
36. Petukhov A. G. · Phys. Rev. B: Condens. Matter Mater. Phys. · 2000 · 62 · 52010.1103/PhysRevB.62.520 ↗
37. Yanata K. · J. Appl. Phys. · 1993 · 73 · 459510.1063/1.352750 ↗
38. Guyot-Sionnest P. · J. Phys. Chem. Lett. · 2012 · 3 · 116910.1021/jz300048y ↗
39. Prodanovic N. · J. Phys. Chem. Lett. · 2014 · 5 · 133510.1021/jz500086c ↗
40. Ouyang M. · Science · 2003 · 301 · 107410.1126/science.1086963 ↗